Bioassay of 1,2-dichloroethane for possible carcinogenicity.

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Abstract

A bioassay of technical-grade 1,2-dichloroethane for possible carcinogenicity was conducted using Osborne-Mendel rats and B6C3F1 mice. 1,2-Dichloroethane in corn oil was administered by gavage, at either of two dosages, to groups of 50 male and 50 female animals of each species. The 78-week period of chemical administration was followed by an observation period of 32 weeks for the low dose rats of both sexes. The last high dose male rat died after 23 weeks of observation and the last high dose female rat died after 15 weeks of observation. All treated groups of mice were observed for an additional 12 or 13 weeks following chemical administration. Initial dosage levels for the chronic bioassay were selected on the basis of a preliminary subchronic toxicity test. Subsequent dosage adjustments were made during the course of the chronic bioassay. The time-weighted average high and low doses of 1,2-dichloroethane in the chronic study were 95 and 47 mg/kg/day, respectively, for rats of both sexes. The high and low time-weighted average doses for the male mice were 195 and 97 mg/kg/day, respectively, and 299 and 149 mg/kg/day, respectively, for the female mice. For each species, 20 animals of each sex were placed on test as vehicle controls. These animals were gavaged with corn oil at the same times that dosed animals were gavaged with the 1,2-dichloroethane mixtures. Twenty animals of each sex were placed on test as untreated controls for each species. These animals were not intubated. A statistically significant positive association between dosage and the incidence of squamous-cell carcinomas of the forestomach and hemangiosarcomas of the circulatory system occurred in the male rats, but not in the females. There was also a significantly increased incidence of adenocarcinomas of the mammary gland in female rats. The incidences of mammary adenocarcinomas in female mice were statistically significant. There was a statistically significant positive association between chemical administration and the combined incidences of endometrial stromal polyps and endometrial stromal sarcomas in female mice. The incidence of alveolar/bronchiolar adenomas in both male and female mice was also statistically significant. Under the conditions of this study, 1,2-dichloroethane was carcinogenic to Osborne-Mendel rats, causing squamous-cell carcinomas of the forestomach, hemangiosarcomas, and subcutaneous fibromas in male rats and causing mammary adenocarcinomas in female rats. This compound was also found to be carcinogenic to B6C3F1 mice, causing mammary adenocarcinomas and endometrial tumors in female mice, and causing alveolar/bronchiolar adenomas in mice of both sexes.

1,2-二氯乙烷可能致癌性的生物测定。
用奥斯本-孟德尔大鼠和B6C3F1小鼠进行了技术级1,2-二氯乙烷可能致癌性的生物测定。将玉米油中的1,2-二氯乙烷以两种剂量中的任意一种灌胃给每组50只雄性和50只雌性动物。给药78周后,对低剂量大鼠和雌雄大鼠进行32周的观察。最后一只高剂量雄性大鼠观察23周后死亡,最后一只高剂量雌性大鼠观察15周后死亡。所有治疗组小鼠在给药后再观察12或13周。慢性生物试验的初始剂量水平是根据初步的亚慢性毒性试验选择的。随后的剂量调整是在慢性生物测定过程中进行的。在慢性研究中,1,2-二氯乙烷的时间加权平均高剂量和低剂量分别为95和47 mg/kg/d。雄性小鼠的高、低时间加权平均剂量分别为195、97 mg/kg/d,雌性小鼠的高、低时间加权平均剂量分别为299、149 mg/kg/d。每个物种各取20只雌雄动物作为对照进行试验。这些动物用玉米油灌胃,同时用1,2-二氯乙烷混合物灌胃。每种性别各20只动物作为未处理的对照进行试验。这些动物没有插管。剂量与前胃鳞状细胞癌和循环系统血管肉瘤的发病率之间有统计学意义的正相关,发生在雄性大鼠身上,而在雌性大鼠身上则没有。雌性大鼠的乳腺腺癌发病率也显著增加。雌性小鼠乳腺腺癌的发生率有统计学意义。在雌性小鼠中,化学药物给药与子宫内膜间质息肉和子宫内膜间质肉瘤的联合发病率有统计学意义的正相关。雌雄小鼠肺泡/细支气管腺瘤的发生率也有统计学意义。在本研究条件下,1,2-二氯乙烷对奥斯本-孟德尔大鼠具有致癌性,雄性大鼠可引起前胃鳞状细胞癌、血管肉瘤和皮下纤维瘤,雌性大鼠可引起乳腺腺癌。该化合物还被发现对B6C3F1小鼠具有致癌性,在雌性小鼠中引起乳腺腺癌和子宫内膜肿瘤,在两性小鼠中引起肺泡/细支气管腺瘤。
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